Furukawa S, Kamo I, Furukawa Y, Akazawa S, Satoyoshi E, Itoh K, Hayashi K
J Neurochem. 1983 Mar;40(3):734-44. doi: 10.1111/j.1471-4159.1983.tb08040.x.
A sensitive two-site enzyme immunoassay system for mouse beta nerve growth factor (NGF) was developed, based on the sandwiching of the antigen between anti-mouse beta NGF antibody IgG coated to a polystyrene tube and anti-mouse beta NGF antibody Fab'-linked beta-D-galactosidase (beta-D-galactoside hydrolase, EC 3.2.1.23). This method has the following advantages: (a) the procedures are simple and rapid compared to bioassay or two-site radioimmunoassay; (b) antibody Fab'-beta-D-galactosidase complex is more stable than 125I-labeled antibody; (c) purified beta NGF is detectable at a concentration as low as 10 pg/ml. Our enzyme immunoassay was used to examine the levels of NGF in some tissues of mice. The submaxillary gland contained a high concentration of NGF. However, other tissues, such as the heart, brain, and skeletal muscle, and serum did not contain detectable NGF. These results support recent findings by other investigators that NGF was not found in the organs/tissues other than the submaxillary gland of mice.
基于包被于聚苯乙烯管上的抗小鼠β神经生长因子(NGF)抗体IgG与抗小鼠βNGF抗体Fab'-连接的β-D-半乳糖苷酶(β-D-半乳糖苷水解酶,EC 3.2.1.23)之间夹着抗原,开发了一种用于小鼠β神经生长因子(NGF)的灵敏双位点酶免疫分析系统。该方法具有以下优点:(a)与生物测定法或双位点放射免疫测定法相比,操作简单快速;(b)抗体Fab'-β-D-半乳糖苷酶复合物比125I标记的抗体更稳定;(c)纯化的βNGF在低至10 pg/ml的浓度下即可检测到。我们的酶免疫分析法用于检测小鼠某些组织中的NGF水平。颌下腺含有高浓度的NGF。然而,其他组织,如心脏、大脑和骨骼肌以及血清中未检测到NGF。这些结果支持了其他研究者最近的发现,即在小鼠颌下腺以外的器官/组织中未发现NGF。